Align Acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate BWI76_RS23710 BWI76_RS23710 acetyl-CoA acetyltransferase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_2411 (393 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS23710 BWI76_RS23710 acetyl-CoA acetyltransferase Length = 396 Score = 362 bits (929), Expect = e-104 Identities = 196/389 (50%), Positives = 254/389 (65%), Gaps = 2/389 (0%) Query: 5 EIYVVSAARTAIGTFGGSLKDVPLADLATTAVKAALERAAVDPALVGHLVMGNVIPTETR 64 +I VVS RTAIGTF GSLK DL ++ A+ RA + P + ++GNV Sbjct: 6 DIVVVSGVRTAIGTFNGSLKHTHQHDLGAAVIREAVNRAGLAPQDIDETIVGNVGQI-AE 64 Query: 65 DAYISRVAAMNAGIPKETPAYNVNRLCGSGLQAIINAAQTLMLGDADIVVGAGAESMSRG 124 +I+R+ + AGIP+E+ AY+VNR CGSGLQA+ + L G A++VV G E+M++ Sbjct: 65 SGFIARICQLRAGIPQESTAYSVNRQCGSGLQALADGMMQLQSGQAEVVVACGTENMTQL 124 Query: 125 PYLMPAARWGSRMGNAQVIDYMLGILHDPFHGIHMGITAENVAARNGITREMQDALAFED 184 PY + AR G RMG+ ++ D ++ IL P H GITAENVA R GITRE D A+ Sbjct: 125 PYYLRKARDGYRMGHGELEDGLISILTWPEGPYHNGITAENVAQRFGITREAMDDFAWSS 184 Query: 185 QQRAAHAIANGYFSEQIATVEIQD-RKGVKLFSVDEHPRATSLEQLAAMKPAFKKDGSVT 243 QQ+A AIA F EQI +E+ D +K +LF+ DEHPR T E+LAA++PAFK DG VT Sbjct: 185 QQKALKAIAEERFREQILALEVPDGKKATRLFATDEHPRDTPREKLAALRPAFKADGVVT 244 Query: 244 AGNASGLNDGAAALVMASGNAVQANNLKPLARLVSYAHAGVEPEFMGLGPIPATRLALKR 303 A N+SG+NDGAAALVM + + L P R+ +A AG E MG GP PATR + R Sbjct: 245 AANSSGINDGAAALVMMTRQQAEKRGLTPRMRIRGWAVAGCGAEIMGFGPSPATRRLMDR 304 Query: 304 AGLTVADLDVIEANIAFAAQACAVSQELDLDPAKVNPNGSGIALGHPVGATGAIIATKAI 363 + V +D+IE N AFAAQA AV +L LDPA+VN NG IALGHPVGA+GAI+ K + Sbjct: 305 LNMDVHAIDLIELNEAFAAQALAVMNDLRLDPARVNVNGGAIALGHPVGASGAILPVKLM 364 Query: 364 HELHRTGGRYALVTMCIGGGQGIAAIFER 392 +E+ R+G R LVTMCIGGGQGI+ +FER Sbjct: 365 YEMARSGARTGLVTMCIGGGQGISMLFER 393 Lambda K H 0.318 0.133 0.378 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 414 Number of extensions: 17 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 393 Length of database: 396 Length adjustment: 31 Effective length of query: 362 Effective length of database: 365 Effective search space: 132130 Effective search space used: 132130 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory